Canonical Allele Identifier: CA414810651
Gene: MT-ND4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.11648G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.11648G>C , J01415.2:m.11648G>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361381.2:c.889G>C ENSP00000354961.2:p.Val297Leu
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